HGVS | Genome Assembly |
---|---|
NC_000010.11:g.122461671del , CM000672.2:g.122461671del | GRCh38 |
NC_000010.10:g.124221187del , CM000672.1:g.124221187del | GRCh37 |
NC_000010.9:g.124211177del | NCBI36 |
NG_011554.1:g.5147del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368984.8:c.19del MANE Select | ENSP00000357980.3:p.Ala7LeufsTer? | |
ENST00000648167.1:c.154+2962del | ENSP00000498033.1:n.154+2962del | |
ENST00000368984.7:c.19del | ENSP00000357980.3:p.Ala7LeufsTer? | |
NM_002775.4:c.19del | NP_002766.1:p.Ala7LeufsTer? | |
NM_002775.5:c.19del MANE Select | NP_002766.1:p.Ala7LeufsTer? |